HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-5-chloropyridine-4-carboxaldehyde → HCID 86645357, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-5-chloropyridine-4-carboxaldehyde | HCID 73012613 | — |
| Reactant | HCID 86645358 | HCID 86645358 | — |
| Reactant | HCID 178527881 | HCID 178527881 | — |
| Solvent | 2,4-Dichloropyridine | HCID 33515 | — |
| Product | HCID 86645357 | HCID 86645357 | — |
Reaction Steps
Introduction of the formyl group in 2,4-dichloro-pyridine according to the synthesis of 3-bromo-5-chloro-pyridine-4-carbaldehyde and subsequent reaction with thiazole-2-thiol according to the synthesis of 3-chloro-5-(thiazol-2-ylsulfanyl)-pyridine-4-carbaldehyde yielded the title compound. MS (m/z): 257.2 [H+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410134B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-ee1eb291b2d740afb2c69f64092ee720 |
| Source note | uspto-grants-2013_04 |